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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509930Generated: October 27, 2026

N-Iodosuccinimide → 5-iodo-4-methyl-7H-pyrrolo[2,3-d]pyrimidine

https://huagongshe.com/reaction/509930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant4-Methyl-7H-pyrrolo(2,3-d)pyrimidineHCID 51341959—
SolventDichloromethaneHCID 6344—
Product5-iodo-4-methyl-7H-pyrrolo[2,3-d]pyrimidineHCID 5825929976.2%

Reaction Steps

To 4-methyl-7H-pyrrolo[2,3-d]pyrimidine (18, 0.634 g, 4.76 mmol) in 50 mL of dichloromethane, N-iodosuccinimide (1.3 g, 5.7 mmol) was added and the reaction stirred at room temperature for 45 minutes. The reaction was concentrated under vacuum, then ethyl acetate was added and washed with 1 N aqueous sodium thiosulfate. The organic layer was dried over sodium sulfate, filtered and the filtrate concentrated under vacuum. The resulting material was purified by silica gel column chromatography, eluting with 20-100% ethyl acetate in hexane. Appropriate fractions were combined and concentrated under vacuum to provide the desired compound (19, 0.94 g). MS (ESI) [M+H+]+=260.26.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096593B2
Source datasetuspto-grants-2015_08
ORD IDord-96a101577cbc4cb9bc9cede27d7906fd
Source noteuspto-grants-2015_08